A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674533



Internal ID15064499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58305116..58339641hg38UCSC Ensembl
Innerchr17:56382477..56417002hg19UCSC Ensembl
Innerchr17:53737476..53772001hg18UCSC Ensembl
Innerchr17:53737476..53772001hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3834526
hg1934526
hg1834526
hg1734526
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517229
Supporting Variants
Samples
Known GenesBZRAP1, BZRAP1-AS1, MIR142, MIR4736
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674533
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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